ctDNA-guided Therapy Optimization in Newly Diagnosed DLBCL

Not Applicable

Recruiting

• Conditions: Lymphoma; Lymphoma, B-Cell; Diffuse Large B Cell Lymphoma; Diffuse Large B-Cell Lymphoma, Not Otherwise Specified; High-grade B-cell Lymphoma

• Registration Number: NCT06693830
• Lead Sponsor: Hua-Jay J Cherng, MD

Brief Summary

The purpose of this study is to 1) determine whether it is feasible to measure circulating tumor DNA (ctDNA) in real-time during standard treatment for newly diagnosed diffuse large B-cell lymphoma (DLBCL), and 2) evaluate the outcomes of participants with undetectable ctDNA in the middle of treatment who receive a shortened course of chemotherapy.

There are no investigational drug agents to be administered in this study. The investigational assay, phased variant enrichment and detection sequencing (PhasED-seq) will be used to guide de-escalation of standard-of-care therapy for newly diagnosed DLBCL.

The PhasED-seq assay has not yet been approved by the Food and Drug Administration (FDA).

Detailed Description

The feasibility of real-time ctDNA sequencing with PhasED-seq during DLBCL therapy has yet to be established. There are logistical challenges to developing a consistent and efficient workflow for obtaining, processing, and sequencing patient samples during frontline immunochemotherapy. ctDNA sequencing must be reliable with a low failure rate before it can be adopted as an integral biomarker for treatment decision making in the clinic. Furthermore, the outcomes of patients who have undetectable ctDNA with PhasED-seq during treatment who de-escalate their chemotherapy must be assessed.

In this study an anticipated 40 patients with newly diagnosed DLBCL will be screened for a target enrollment goal of 32 participants. These 32 patients will receive standard treatment with 4 cycles of R-CHOP or R-pola-CHP immunochemotherapy. These patients will have blood samples collected after 3 cycles to test for the presence of ctDNA in real-time. Patients who have successful real-time sequencing and have undetected ctDNA as well as a complete remission on interim re-staging scans will de-escalate treatment and omit chemotherapy for their final 2 cycles of treatment. These patients will receive rituximab alone for their final 2 cycles. All others will continue standard treatment.

26 participants are expected to have successful real-time sequencing, of which 13 patients are expected to meet criteria for treatment de-escalation and omit chemotherapy for their final 2 cycles of treatment.

Study Timeline

• Study First Submitted: 2024-11-15
• Study First Submitted QC: 2024-11-15
• Study First Posted: 2024-11-18
• Study Start: 2024-12-11
• Status Verified: 2025-01
• Last Update Submitted: 2025-01-14
• Last Update Posted: 2025-01-16
• Primary Completion: 2027-12
• Study Completion: 2029-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

1. Patients with newly diagnosed, histologically confirmed CD20+ DLBCL

   • Stage II-IV disease
   • Planned for anthracycline-based therapy with standard dosed R-CHOP or R-pola- CHP without consolidative radiation
   • Measurable disease on cross sectional imaging ≥ 1.5 cm in longest diameter and measurable in two perpendicular dimensions, with at least one corresponding hypermetabolic lesion by Lugano classification on baseline FDG PET/CT or CT with intravenous contrast of the chest, abdomen, and pelvis if FDG PET/CT not available.

2. Age 18 years or older at time of screening

3. Subject/legal representative willing and able to provide written informed consent

4. Ability to comply with outpatient treatment, laboratory monitoring, and required clinic visits for duration of study participation

5. Organ function as assessed by laboratory and cardiac function testing and Eastern Cooperative Oncology Group (ECOG) performance status in appropriate range for receipt of R-CHOP or R-pola-CHP at standard dose as per treating physician

Exclusion Criteria

1. Previous treatment for diffuse large B-cell lymphoma, except as outlined below:

   • Up to 14 days of corticosteroids for the relief of lymphoma-related symptoms
   • A dose of pre-phase vincristine or rituximab
   • One cycle of R-chemotherapy (including but not limited to R-CHOP, R-pola-CHP, dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, rituximab [DA-EPOCH-R) that has not started more than 28 days prior to consent
   • Intrathecal chemotherapy for central nervous system (CNS) prophylaxis
   • Radiation therapy for the treatment or prevention of spinal cord compression that has not started more than 28 days prior to enrollment

2. Simultaneous participation in other treatment clinical protocol

3. Planned anti-lymphoma therapies beyond R-CHOP or R-pola-CHP:

   • Consolidative radiation to any baseline sites of disease

   • Planned high-dose intravenous methotrexate for central nervous system (CNS) lymphoma prophylaxis (both mid-cycle and EOT excluded)

     • Any number of doses of intrathecal chemotherapy for CNS lymphoma prophylaxis are allowed

4. Transformed indolent lymphoma (including follicular lymphoma, marginal zone lymphoma, or lymphoplasmacytic lymphoma) or grade IIIB follicular lymphoma

5. Known CNS involvement by lymphoma. R-CHOP and R-pola- CHP are insufficient to treat CNS disease.

6. Any disease characteristics that would make R-CHOP or R-pola-CHP without radiation insufficient therapy at the discretion of the treating physician

   • High-grade B-cell lymphoma with rearrangement of MYC and BCL2, primary mediastinal B-cell lymphoma, and HIV-associated lymphomas are excluded

7. Richter transformation of chronic lymphocytic leukemia

8. Pregnancy and/or nursing period. R-CHOP and R-pola-CHP may cause fetal harm or birth defects, and effects of exposure in the breastfed infant are unknown.

   • A person who has had menses at any time in the preceding 12 consecutive months or who has semen likely to contain sperm is considered to be of "childbearing potential"
   • Women of childbearing potential are eligible if a negative serum or urine beta human chorionic gonadotropin pregnancy test is documented within 28 days of screening, and they must agree to us an effective contraception method during systemic treatment
   • Men who have partners of childbearing potential must agree to use an effective contraceptive method during systemic treatment
   • In addition to routine contraceptive methods, "acceptable contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) including hysterectomy, bilateral oophorectomy, bilateral tubal ligation/occlusion, and vasectomy with testing showing no sperm in the semen.

9. Uncontrolled active systemic infection

   • Patients with a positive hepatitis B virus (HBV) core antibody and negative HBV surface antigen consistent with prior HBV exposure must be willing to take appropriate anti-viral prophylaxis.
   • Patients with evidence of chronic HBV infection must have undetectable HBV viral load on the most recent test results obtained within the last year and received suppressive therapy.
   • Participants with a history of hepatitis C virus (HCV) infection must have an undetectable viral load. Participants currently being treated for HCV infection must have undetectable HCV viral load test on the most recent test results obtained within 28 days prior to consent.

10. Active second malignancy unless in remission and with life expectancy > 2 years with exception of patients diagnosed with basal cell or squamous cell carcinoma of the skin or carcinoma "in situ" of the cervix or breast who are eligible even if diagnosed within 2 years. If patients have another malignancy that was treated within the last 2 years, such patients may be enrolled, if the likelihood of requiring systemic therapy for this other malignancy within 2 years is less than 10%, as determined by an expert in that particular malignancy at CUIMC, and after consultation with the Principal Investigator. Hormone therapy for treated prostate and breast cancer is allowed.

11. Known hypersensitivity to any component of R-CHOP or R-pola-CHP

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SEQUENTIAL

Primary Outcome Measures

Name	Time	Method
Success Rate of Real-Time Circulating Tumor DNA (ctDNA) Sequencing	up to 5 months	Success defined as: C4D1 sample collected, DNA successfully sequenced from the diagnostic tissue sample, C4D1 timepoint result must be available within 28 days of C4D1
Complete Response Rate (CRR)	up to 6 months	Complete response rate as assessed by PET/CT scan in participants who receive de-escalated treatment

Secondary Outcome Measures

Name	Time	Method
Rate of Minimal Residual Disease (MRD) Negativity	Up to 4 months	MRD negativity defined as ctDNA negativity as determined by blood sample analysis
Time to ctDNA Result	Up to 28 days	Time from sample collection to ctDNA result
Proportion of Participants Eligible for De-escalation	Up to 5 months	The proportion of participants eligible for de-escalation
Progression Free Survival (PFS) Rate	2 years	PFS defined as the time between C1D1 of therapy and progression of DLBCL.
Overall Survival (OS) Rate	2 years	OS defined as the time between C1D1 of therapy and death from any cause.

Trial Locations

Locations (1)

Columbia University; 🇺🇸 New York, New York, United States